Principal Investigator (Clinical Research Physician) - Charlotte, NC 245987

Medix

Charlotte, NCFull-timePosted Mar 29, 2026

240K–270K a year

Behavioral Health Market Context

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Job Description

le and supportive environment.

Job Responsibilities: Key Responsibilities:

Serve as the Principal Investigator on clinical trials across multiple therapeutic areas

Conduct medical evaluations and assessments for study participants

Ensure compliance with FDA, GCP, and other regulatory requirements

Review and approve essential study documents, including informed consent forms and medical histories

Oversee participant safety and manage adverse events with the research team

Collaborate with sponsors, CROs, and internal staff to meet study goals and timelines

Provide medical oversight to coordinators and research personnel

Contribute to identifying and developing new clinical trial opportunities
Qualifications: Qualifications

MD or DO with Board Certification or Eligibility in Internal Medicine, Family Medicine, or a related field

Active North Carolina medical license (or ability to obtain)

Clinical experience in general medicine; clinical research experience is a plus but not required

Solid understanding of clinical diagnostics, pharmacology, and patient care standards

Strong communication and leadership skills

Commitment to ethical research practices and patient safety
Working Hours: Full Time

Mon - Fri 8 AM - 5 PM

Qualifications

  • MD or DO with Board Certification or Eligibility in Internal Medicine, Family Medicine, or a related field
  • Active North Carolina medical license (or ability to obtain)
  • Solid understanding of clinical diagnostics, pharmacology, and patient care standards
  • Strong communication and leadership skills
  • Commitment to ethical research practices and patient safety

Benefits

    Responsibilities

    • Serve as the Principal Investigator on clinical trials across multiple therapeutic areas
    • Conduct medical evaluations and assessments for study participants
    • Ensure compliance with FDA, GCP, and other regulatory requirements
    • Review and approve essential study documents, including informed consent forms and medical histories
    • Oversee participant safety and manage adverse events with the research team
    • Collaborate with sponsors, CROs, and internal staff to meet study goals and timelines
    • Provide medical oversight to coordinators and research personnel
    • Contribute to identifying and developing new clinical trial opportunities
    • Working Hours: Full Time


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